Literature DB >> 25593020

In situ activation of benzyl alcohols with XtalFluor-E: formation of 1,1-diarylmethanes and 1,1,1-triarylmethanes through Friedel-Crafts benzylation.

Justine Desroches1, Pier Alexandre Champagne, Yasmine Benhassine, Jean-François Paquin.   

Abstract

The Friedel-Crafts benzylation of arenes using benzyl alcohols activated in situ with XtalFluor-E is described. A wide range of 1,1-diarylmethanes and 1,1,1-triarylmethanes were prepared under experimentally simple and mild conditions, without the need for a transition metal or a strong Lewis acid. Notably, the reactivity observed demonstrates the potential of XtalFluor-E to induce C-OH bond ionization and SN1 reactivity of benzylic alcohols.

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Year:  2015        PMID: 25593020     DOI: 10.1039/c4ob02655a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  XtalFluor-E® mediated proto-functionalization of N-vinyl amides: access to N-acetyl N,O-acetals.

Authors:  Y Yi; H Gholami; M G Morrow; B Borhan
Journal:  Org Biomol Chem       Date:  2017-11-22       Impact factor: 3.876

  1 in total

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